Answer:
the child in custody could not be the missing child
Step-by-step explanation:
Hemophilia is a sex-linked recessive disorder, which means it’s carried on the X chromosome. Males have one X and one Y chromosome (XY), and females have two X chromosomes (XX). If a male inherits the X chromosome carrying the disorder from his mother, he will have hemophilia. A female would need to inherit two copies of the gene to have the disorder, one from each parent.
In your scenario, the grandfather has hemophilia, which means he carries the gene on his X chromosome. His daughter (the mother of the missing child) would have received this X chromosome, making her a carrier of the trait, even though she doesn’t show symptoms of the disorder.
The mother can pass on the X chromosome carrying the hemophilia gene to her children. If the child in custody is a girl (as indicated by the shaded circle), she would need to inherit the gene from both parents to have the disorder. However, the father does not have hemophilia, so he cannot pass on the gene. Therefore, the child in custody could not be the missing child based on the information provided.
Please note that this analysis assumes complete penetrance of the gene, no new mutations, and no non-paternity events. In real-world scenarios, genetic testing would be necessary to confirm these findings.